Linked Data
dbSNP Id:
rs1299911303
gnomAD v2:
7-150883511-G-A
gnomAD v3:
7-151186424-G-A
gnomAD v4:
7-151186424-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.151186424G>A , CM000669.2:g.151186424G>A | GRCh38 |
| NC_000007.13:g.150883511G>A , CM000669.1:g.150883511G>A | GRCh37 |
| NC_000007.12:g.150514444G>A | NCBI36 |
| NG_017016.1:g.6409C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000420175.3:c.552C>T MANE Select | ENSP00000391137.2:p.Pro184= | |
| ENST00000275838.5:c.552C>T | ENSP00000275838.1:p.Pro184= | |
| ENST00000377867.7:c.507C>T | ENSP00000367098.3:p.Pro169= | |
| ENST00000420175.2:c.552C>T | ENSP00000391137.2:p.Pro184= | |
| NM_001142459.1:c.552C>T | NP_001135931.2:p.Pro184= | |
| NM_001142460.1:c.552C>T | NP_001135932.2:p.Pro184= | |
| NM_080871.3:c.507C>T | NP_543147.2:p.Pro169= | |
| XM_005249949.3:c.687C>T | XP_005250006.1:p.Pro229= | |
| NM_001142459.2:c.552C>T MANE Select | NP_001135931.2:p.Pro184= | |
| NM_080871.4:c.507C>T | NP_543147.2:p.Pro169= |